Department of Infectious Diseases and Clinical Microbiology, Faculty of Medicine, Erciyes University, Kat 10, Melikgazi, 38039, Kayseri, Turkey.
Infection. 2010 Jun;38(3):217-21. doi: 10.1007/s15010-010-0003-6. Epub 2010 Mar 17.
The aim of this study was to investigate the interaction between intravenous piperacillin/tazobactam treatment and Aspergillus galactomannan antigen (GM) and 1,3-beta-D: -glucan (BDG) test results in patients without known risk factors for invasive fungal infections (IFI).
Patients without known risk factors for IFI and who were to receive piperacillin/tazobactam monotherapy were considered eligible for the study. Serum samples were obtained both before and after antibiotic infusion on the first, third, seventh and tenth days of a piperacillin/tazobactam treatment course and 4 days after the last dose. GM was determined by Platelia Aspergillus ELISA (Bio-Rad Laboratories) and BDG was assayed using the Fungitell kit (Associates of Cape Cod, East Falmouth, MA) according to manufacturers' specifications.
A total of 135 serum samples were collected from 15 patients. When a cut-off level of >or=0.7 was used for GM positivity, there were no false positive results. When a cut-off level of >or=0.5 was used, six serum samples were positive. There were no statistically significant differences between the median GM indices or median BDG levels of the various sampling times. However, 24 of 135 serum samples were positive for BDG for a threshold of 80 pg/mL. After ruling out fungal infections and all known potential causes of false BDG positivity, environmental contamination remained a possible cause of BDG reactivity.
No significant interaction was observed between piperacillin/tazobactam administration and Aspergillus GM and BDG assays. Positive results for these tests should be evaluated cautiously in patients at high risk for IFI receiving piperacillin/tazobactam.
本研究旨在探讨无明确侵袭性真菌感染(IFI)危险因素的患者静脉滴注哌拉西林/他唑巴坦治疗与曲霉菌半乳甘露聚糖抗原(GM)和 1,3-β-D:-葡聚糖(BDG)检测结果之间的相互作用。
符合纳入标准的患者为无明确 IFI 危险因素且接受哌拉西林/他唑巴坦单药治疗的患者。在哌拉西林/他唑巴坦治疗疗程的第 1、3、7 和 10 天以及最后一次给药后 4 天,分别在抗生素输注前后采集血清样本。采用 Platelia Aspergillus ELISA(Bio-Rad Laboratories)检测 GM,按照制造商的说明书使用 Fungitell 试剂盒(Associates of Cape Cod,East Falmouth,MA)检测 BDG。
共采集了 15 例患者的 135 份血清样本。当 GM 阳性的截断值为 >or=0.7 时,没有假阳性结果。当截断值为 >or=0.5 时,6 份血清样本呈阳性。在不同采样时间,GM 指数中位数或 BDG 水平中位数之间无统计学差异。然而,当 BDG 的阈值为 80 pg/mL 时,有 24 份血清样本呈阳性。在排除真菌感染和所有已知的潜在 BDG 假阳性原因后,环境污染仍然是 BDG 反应性的一个可能原因。
哌拉西林/他唑巴坦给药与曲霉菌 GM 和 BDG 检测之间未观察到明显的相互作用。在接受哌拉西林/他唑巴坦治疗且 IFI 风险较高的患者中,应谨慎评估这些检测的阳性结果。